Canonical Allele Identifier: CA414806352
Gene: MT-ND4L HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.10677G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10677G>C , J01415.2:m.10677G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.208G>C ENSP00000354728.1:p.Glu70Gln
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